01 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
01 1Verapamil Hydrochloride
01 1Italy
Registration Number : 230MF10106
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2018-08-08
Latest Date of Registration : 2018-08-08
A Verapamil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Verapamil Hydrochloride, including repackagers and relabelers. The FDA regulates Verapamil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Verapamil Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Verapamil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Verapamil Hydrochloride supplier is an individual or a company that provides Verapamil Hydrochloride active pharmaceutical ingredient (API) or Verapamil Hydrochloride finished formulations upon request. The Verapamil Hydrochloride suppliers may include Verapamil Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Verapamil Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Verapamil Hydrochloride Drug Master File in Japan (Verapamil Hydrochloride JDMF) empowers Verapamil Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Verapamil Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Verapamil Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Verapamil Hydrochloride suppliers with JDMF on PharmaCompass.
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